Published in Hum Mol Genet on December 15, 2001
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The leukemogenic CALM/AF10 fusion protein alters the subcellular localization of the lymphoid regulator Ikaros. Oncogene (2007) 1.00
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SALL4 deletions are a common cause of Okihiro and acro-renal-ocular syndromes and confirm haploinsufficiency as the pathogenic mechanism. J Med Genet (2004) 0.92
Mechanisms of small ring formation suggested by the molecular characterization of two small accessory ring chromosomes derived from chromosome 4. Am J Hum Genet (1995) 0.92
The novel CALM interactor CATS influences the subcellular localization of the leukemogenic fusion protein CALM/AF10. Oncogene (2006) 0.92
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Characterization of marker chromosomes by microdissection and fluorescence in situ hybridization. Prenat Diagn (1994) 0.83
C-terminally truncated kindlin-1 leads to abnormal adhesion and migration of keratinocytes. Br J Dermatol (2008) 0.83
A guideline for simulation studies of wastewater treatment plants. Water Sci Technol (2004) 0.83
Mapping the diabetes polygene Idd3 on mouse chromosome 3 by use of novel congenic strains. Mamm Genome (1995) 0.82
AF10 is split by MLL and HEAB, a human homolog to a putative Caenorhabditis elegans ATP/GTP-binding protein in an invins(10;11)(p12;q23q12). Blood (1996) 0.82
Identification of novel and known KRT5 and KRT14 mutations in 53 patients with epidermolysis bullosa simplex: correlation between genotype and phenotype. Br J Dermatol (2010) 0.82
Unique family with Townes-Brocks syndrome, SALL1 mutation, and cardiac defects. Am J Med Genet (2001) 0.82
Phenotypic spectrum of epidermolysis bullosa associated with α6β4 integrin mutations. Br J Dermatol (2013) 0.82
[Okihiro syndrome : Duane's syndrome and radial malformations of the limbs]. Ophthalmologe (2008) 0.81
Detection of CDKN2 deletions in tumor cell lines and primary glioma by interphase fluorescence in situ hybridization. Cancer Res (1995) 0.81
Lethal junctional epidermolysis bullosa with pyloric atresia due to compound heterozygosity for two novel mutations in the integrin β4 gene. Klin Padiatr (2011) 0.81
Clinical and molecular cytogenetic studies of a large de novo interstitial deletion 16q11.2-16q21 including the putative transcription factor gene SALL1. J Med Genet (2000) 0.80
Association of Jacobsen syndrome and bipolar affective disorder in a patient with a de novo 11q terminal deletion. Am J Med Genet A (2006) 0.80
Refined mapping of genomic rearrangements involving the short arm of chromosome 9 in acute lymphoblastic leukemias and other hematologic malignancies. Blood (1995) 0.79
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AML1-ETO meets JAK2: clinical evidence for the two hit model of leukemogenesis from a myeloproliferative syndrome progressing to acute myeloid leukemia. Leukemia (2007) 0.79
A novel family-specific translocation t(2;20)(p24.1;q13.1) associated with recurrent abortions: molecular characterization and segregation analysis in male meiosis. Cytogenet Genome Res (2002) 0.79
A t(6;12)(q23;p13) results in the fusion of ETV6 to a novel gene, STL, in a B-cell ALL cell line. Genes Chromosomes Cancer (1997) 0.78
Townes-Brocks syndrome and renal dysplasia: a novel mutation in the SALL1 gene. Pediatr Nephrol (2000) 0.78
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Three novel SALL1 mutations extend the mutational spectrum in Townes-Brocks syndrome. J Med Genet (2000) 0.77
New framework for standardized notation in wastewater treatment modelling. Water Sci Technol (2010) 0.77
Identification of pericentric inversion 12, inv(12)(p13.1q11), by fluorescence in situ hybridization in a patient with acute myeloid leukemia (AML-M6). Cancer Genet Cytogenet (1997) 0.77
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A microdissection library of the rat renal carcinoma gene region. Cytogenet Cell Genet (1995) 0.77
FHL2 interacts with CALM and is highly expressed in acute erythroid leukemia. Blood Cancer J (2011) 0.77
Late-onset inversa recessive dystrophic epidermolysis bullosa caused by glycine substitutions in collagen type VII. Br J Dermatol (2011) 0.77
CHD7 mutations causing CHARGE syndrome are predominantly of paternal origin. Clin Genet (2011) 0.77
Dystrophic epidermolysis bullosa pruriginosa is not associated with frequent FLG gene mutations. Br J Dermatol (2008) 0.77
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